NIPA1 Polyclonal Antibody, 100ul Plasma a non-autoimmune condition

a non-autoimmune condition

There are at least two isozymes of the corticosteroid 11-beta-dehydrogenase

Mutations of this gene result in factor X deficiency

The alpha chain is approximately 33-35 kDa

The encoded membrane protein acts as a receptor for neuropeptide S and affects a variety of cellular processes through its signaling

NIPA1 Polyclonal Antibody, 100ul Plasma a non-autoimmune conditionThis gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6.